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FDA Inspection
•REVIN LABS PRIVATE LIMITED•January 25, 2023

REVIN LABS PRIVATE LIMITED – FDA Inspection, Jan 25, 2023

Record Details

This FDA Inspection record concerns REVIN LABS PRIVATE LIMITED, with an inspection on January 25, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
REVIN LABS PRIVATE LIMITED
Inspection Date
January 25, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Saied A. Asbagh (FDA Associated Person)
View Company Profile

ID · 317267d8-03f4-4bbe-8c5a-5ffd4cb2bd29

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1196673
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 211.165(e)Test methods
  2. 21 CFR 211.22(d)Procedures not in writing, fully followed
  3. 21 CFR 211.25(a)Training--operations, GMPs, written procedures

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